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dS Flex Coil M 1.5T

EUDAMED

Class IIb (EU MDR)

Ref 45980085495X

by Philips Healthcare (Suzhou) Co., Ltd.

Identity

Trade Name
dS Flex Coil M 1.5T EUDAMED
Device Name
Prodiva 1.5T EUDAMED
Model / Reference
45980085495X EUDAMED

Identifiers

Primary DI / UDI-DI
00884838083776 EUDAMED
Basic UDI-DI
0884838BM288TC EUDAMED
Direct Marketing DI
00884838083776 EUDAMED
EMDN Code
Z1105018001 MAGNETIC RESONANCE (MR) RADIOFREQUENCY SURFACE COILS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: MRI system coil, radio-frequency

dS Flex Coil M 1.5T by Philips Healthcare (Suzhou) Co., Ltd. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as MRI system coil, radio-frequency.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000003923
Authorised Representative
Philips Medical Systems Nederland B.V. NL-AR-000001422

Sources (1)

  • EUDAMED 1622f5bd-84c7-4939-9aec-549fbabd71f3 61 fields · synced Jul 21, 2026